Canonical Allele Identifier: CA337737541
Gene: ANOS2P HGNC NCBI

Linked Data

dbSNP Id: rs112983888
gnomAD v3: Y-13739397-A-G
gnomAD v4: Y-13739397-A-G
MyVariant Identifiers: chrY:g.15851277A>G (hg19) chrY:g.13739397A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13739397A>G , CM000686.2:g.13739397A>G GRCh38
NC_000024.9:g.15851277A>G , CM000686.1:g.15851277A>G GRCh37
NC_000024.8:g.14360671A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000652544.1:n.535-15243A>G
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